CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 168 enrolled
Drug / intervention
PEGASYS +2 moredrug
Likely dose
PEGASYS 45 microgramsfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01259856
NCT01259856Phase 3Completed

Randomized Trial of Pegylated Interferon Alfa-2a Versus Hydroxyurea Therapy in the Treatment of High Risk Polycythemia Vera (PV) and High Risk Essential Thrombocythemia (ET)

Ronald Hoffman·interventional·Posted Dec 14, 2010·Updated Apr 30, 2019

In Brief

A Phase 3 clinical trial evaluating PEGASYS, Hydroxyurea, and 1 other intervention for High Risk Polycythemia Vera and High Risk Essential Thrombocythemia. Completed, enrolled 168 participants across 25 sites in 4 countries.

Detailed Summary

This research is looking at two conditions, Essential Thrombocythemia (ET) and Polycythemia Vera (PV). ET causes people to produce too many blood cells called platelets and PV causes too many platelets and red blood cells to be made. Platelets are particles which circulate in the blood stream and normally prevent bleeding and bruising. Having too many platelets in the blood increases the risk of developing blood clots, which can result in life threatening events like heart attacks and strokes. When the number of red blood cells is increased in PV this will slow the speed of blood flow in the body and increases the risk of developing blood clots. The purpose of this study is to look at the effectiveness of giving participants who have been diagnosed with ET or PV one of two different study regimens over time. The study subject will be followed for their condition for about 5 years. The subject will be randomized into one of two study regimens, either Pegylated Interferon Alfa-2a (PEGASYS) or Aspirin and Hydroxyurea (also called Hydroxycarbamide). The subject must be newly diagnosed or already receiving treatment for either PV or ET. Each of the study drugs used in this study is already being used to treat subjects with ET or PV currently, but the investigators are unsure which study drug is better.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance, Italy, United Kingdom, United States

Timeline

Phase 3CompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedDec 14, 2010
Enrollment StartSep 1, 2011
Primary CompletionJun 30, 2017
TodayJul 2, 2026
Enrollment to primary: 5.8 yearsPosted 15.5 years ago

Interventions

PEGASYSdrug

The subject will begin receiving the PEGASYS at a dose level of 45 micrograms weekly and gradually get increased to the maximum dose of 180 micrograms per week. The dose will be administered by prefilled syringes that will be injected subcutaneously. Subjects will receive therapy for up to 12 months.

Hydroxyureadrug

Subjects will receive a 500mg tablet to be taken twice daily for up to 12 months of treatment.

Aspirindrug

Subject will be asked to take 81 to 100mg per day for the 12 months of the study treatment.